Some users have reported complications
April 8, 2025
Bausch + Lomb is recalling intraocular lenses (IOLs) on its enVista platform. This action was taken after the company received reports of complications, the cause of which could not immediately be explained.
As much as we believe in the enVista platform, patient safety will always be our number one priority, Brent Saunders, chairman and CEO, Bausch + Lomb, said in a press release. Surgeons and patients trust Bausch + Lomb, and I believe that this voluntary recall is the best thing we can do to honor that trust.
The recall is in response to an increased number of reports of toxic anterior segment syndrome (TASS), and includes all lots of the following enVista Aspire, enVista Aspire Toric, enVista Envy and enVista Envy Toric, as well as enVista monofocal and enVista monofocal Toric IOL models in the U.S.
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Model Description
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Model Identifier:
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Lots
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UDI-DI
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enVista Monofocal IOL
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All models starting with EE
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ALL
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Click here
External Link Disclaimer
for UDI list
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enVista Aspire IOL
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All models starting with EA
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enVista Envy IOL
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All models starting with EN
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enVista Monofocal Toric IOL
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All models starting with ETE
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enVista Aspire Toric IOL
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All models starting with ETA
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enVista Envy Toric IOL
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All models starting with ETN
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TASS, a potential complication in any cataract surgery, is an inflammatory reaction inside the eye that can have a variety of causes. When it occurs, this complication typically appears 12 48 hours after eye surgery.
All enVista TASS cases reported to Bausch + Lomb to date responded quickly to treatment, and none have required removal of the lens.
These reports represent only 1-2% of implanted lenses, with a positive prognosis for everyone involved, Saunders said. We look forward to identifying a root cause and bringing the enVista platform back to market.
What to do
For Patients: Cataract surgery patients experiencing eye discomfort should contact their eyecare professional immediately.
For Eyecare Professionals: Please continue to closely monitor cataract surgery patients for at least 48 hours after surgery. Please instruct patients with new or worsening symptoms to contact your office immediately.
To report an adverse event, please contact Bausch + Lomb Customer Service at 1-800-338-2020, option 1, or submit a report to U.S. FDAs MedWatch program (call 1-800-332-1088 to request a form). For more information about this recall, please contact Bausch + Lomb Customer Service at 1-800-338-2020, option 9, 8:00 am to 4:30 pm Eastern, Monday through Friday.
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